Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

T Gordon

Showing results (641-650 of 700) with videos related to

Pageof 70
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|October 27, 2012
Differential Ly-6C expression identifies the recruited macrophage phenotype, which orchestrates the regression of murine liver fibrosisPrakash Ramachandran, Antonella Pellicoro, Madeleine A Vernon, et al.
Arthritis and Rheumatism|October 27, 1997
Range of antinuclear antibodies in "healthy" individualsE M Tan, T E Feltkamp, J S Smolen, et al.
Arthritis and Rheumatism|March 24, 1999
A critical evaluation of enzyme immunoassays for detection of antinuclear autoantibodies of defined specificities. I. Precision, sensitivity, and specificityE M Tan, J S Smolen, J S McDougal, et al.
Circulation|April 6, 2021
Primary Outcome Evaluation of a Next-Generation Left Atrial Appendage Closure Device: Results From the PINNACLE FLX TrialSaibal Kar, Shephal K Doshi, Ashish Sadhu, et al.
Reproductive Biomedicine Online|May 6, 2022
PGDIS position statement on the transfer of mosaic embryos 2021D Leigh, D S Cram, S Rechitsky, et al.
Journal of Medical Genetics|November 5, 2011
Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex developmentSabina Benko, Christopher T Gordon, Delphine Mallet, et al.
Human Molecular Genetics|April 9, 2022
Biallelic alterations in PLXND1 cause common arterial trunk and other cardiac malformations in humansAnne Guimier, Loïc de Pontual, Stephen R Braddock, et al.
American Journal of Human Genetics|November 26, 2013
Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark earsChristopher T Gordon, Florence Petit, Peter M Kroisel, et al.
Annals of Surgery|August 11, 2015
Transfusion of cryopreserved packed red blood cells is safe and effective after trauma: a prospective randomized trialMartin A Schreiber, Belinda H McCully, John B Holcomb, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
Novel de novo ZBTB20 mutations in three cases with Primrose syndrome and constant corpus callosum anomaliesCaroline Alby, Lucile Boutaud, Bettina Bessières, et al.
Pageof 70

Showing results (641-650 of 700) with videos related to

Sort By:
Pageof 70
Proceedings of the National Academy of Sciences of the United States of America|October 27, 2012
Differential Ly-6C expression identifies the recruited macrophage phenotype, which orchestrates the regression of murine liver fibrosisPrakash Ramachandran, Antonella Pellicoro, Madeleine A Vernon, et al.
Arthritis and Rheumatism|October 27, 1997
Range of antinuclear antibodies in "healthy" individualsE M Tan, T E Feltkamp, J S Smolen, et al.
Arthritis and Rheumatism|March 24, 1999
A critical evaluation of enzyme immunoassays for detection of antinuclear autoantibodies of defined specificities. I. Precision, sensitivity, and specificityE M Tan, J S Smolen, J S McDougal, et al.
Circulation|April 6, 2021
Primary Outcome Evaluation of a Next-Generation Left Atrial Appendage Closure Device: Results From the PINNACLE FLX TrialSaibal Kar, Shephal K Doshi, Ashish Sadhu, et al.
Reproductive Biomedicine Online|May 6, 2022
PGDIS position statement on the transfer of mosaic embryos 2021D Leigh, D S Cram, S Rechitsky, et al.
Journal of Medical Genetics|November 5, 2011
Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex developmentSabina Benko, Christopher T Gordon, Delphine Mallet, et al.
Human Molecular Genetics|April 9, 2022
Biallelic alterations in PLXND1 cause common arterial trunk and other cardiac malformations in humansAnne Guimier, Loïc de Pontual, Stephen R Braddock, et al.
American Journal of Human Genetics|November 26, 2013
Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark earsChristopher T Gordon, Florence Petit, Peter M Kroisel, et al.
Annals of Surgery|August 11, 2015
Transfusion of cryopreserved packed red blood cells is safe and effective after trauma: a prospective randomized trialMartin A Schreiber, Belinda H McCully, John B Holcomb, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
Novel de novo ZBTB20 mutations in three cases with Primrose syndrome and constant corpus callosum anomaliesCaroline Alby, Lucile Boutaud, Bettina Bessières, et al.
Pageof 70